Method for halogenation of butyl rubber without using acid neutralizing agent
A technology for halogenating butyl rubber and butyl rubber, applied in the field of halogenation of butyl rubber, can solve the problems of no enlightenment and the like
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Embodiment 1
[0047] Example 1: Bromination of RB301 (with water and caustic). To a solution of RB301 (50 g, 1.6 mol% 1,4-isoprene) in 600 mL hexane was added 45 mL of water. To this mixture was added 0.63 mL of elemental bromine with rapid stirring. After 5 minutes, the reaction mixture was neutralized by introducing a caustic solution prepared by mixing 6.5 mL of aqueous 1.0 M NaOH in 500 mL of water. Immediately following neutralization, 4 ml of stabilizer solution (3.75 g of epoxidized soybean oil and 0.045 g of Irganox 1076 in 100 ml of hexane) were fed to the reaction mixture. The rubber was isolated by steam condensation and dried to constant weight with the aid of a 6" x 12" two-roll mill operating at 100°C. use 1 H nuclear magnetic resonance spectrometer (CDCl 3 ) to measure the microstructure of the obtained material, and the results are listed in Table 1.
Embodiment 2
[0048] Example 2: Bromination of RB301 (without water and caustic). To a solution of RB301 (50 g, 1.6 mol% 1,4-isoprene) in 600 mL of hexane was added 0.63 mL of elemental bromine under rapid stirring. After 5 minutes, 4 ml of stabilizer solution (3.75 g of epoxidized soybean oil and 0.045 g of Irganox 1076 in 100 ml of hexane) were fed to the reaction mixture. The rubber was isolated by steam condensation and dried to constant weight with the aid of a 6" x 12" two-roll mill operating at 100°C. use 1 H nuclear magnetic resonance spectrometer (CDCl 3 ) to measure the microstructure of the obtained material, and the results are listed in Table 1.
Embodiment 3
[0049] Example 3: Bromination of RB402 (without water and caustic). To a solution of RB402 (50 g, 2.0 mol% 1,4-isoprene) in 600 mL of hexane was added 0.63 mL of elemental bromine under rapid stirring. After 5 minutes, 4 ml of stabilizer solution (3.75 g of epoxidized soybean oil and 0.045 g of Irganox 1076 in 100 ml of hexane) were fed to the reaction mixture. The rubber was isolated by steam condensation and dried to constant weight with the aid of a 6" x 12" two-roll mill operating at 100°C. use 1 H nuclear magnetic resonance spectrometer (CDCl 3 ) to measure the microstructure of the obtained material, and the results are listed in Table 1.
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